Phenylation of Platinum(II) Thioether Complexes by Tetraphenylborate(III) in Solid State and Nitromethane Solution
Vadim Yu. Kukushkin, Karin Lövqvist, Bertil Norén, Åke Oskarsson, Lars I. Elding
Abstract
Vadim Yu. Kukushkin, Karin Lövqvist, Bertil Norén, Åke Oskarsson, Lars I. Elding
Abstract
Platinum(II) complexes of the type [Pt(thioether)3Cl]+ (thioether = dimethyl sulfide, thioxane) are capable of abstracting a phenyl group from the BPh− 4 counterion with formation of trans-[Pt(thioether)2ClPh] compounds. Thermal reactions proceed both in the solid phase and in nitromethane solution at elevated temperature and have preparative importance. Phenylation of the Pt(II) centre also occurs in reaction between [Pt(Me2S)2Cl2] and AgBPh4 in CH2Cl2 suspension. Brief X-ray crystallographic structural data for trans-[Pt(Me2S)2ClPh] and [Pt(thioether)3Cl]X (thioether = Me2S, tx, X = SO3CF3; thioether = Me2S, X = PF6) are reported.
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Platinum(II) complexes of the type [Pt(thioether)3Cl]+ (thioether = dimethyl sulfide, thioxane) are capable of abstracting a phenyl group from the BPh− 4 counterion with formation of trans-[Pt(thioether)2ClPh] compounds. Thermal reactions proceed both in the solid phase and in nitromethane solution at elevated temperature and have preparative importance. Phenylation of the Pt(II) centre also occurs in reaction between [Pt(Me2S)2Cl2] and AgBPh4 in CH2Cl2 suspension. Brief X-ray crystallographic structural data for trans-[Pt(Me2S)2ClPh] and [Pt(thioether)3Cl]X (thioether = Me2S, tx, X = SO3CF3; thioether = Me2S, X = PF6) are reported.
Key concepts: Thioether, Nitromethane, Chemistry, Platinum, Counterion, Tetraphenylborate, Medicinal chemistry, Stereochemistry